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Just-in-time Adaptive Feedback Systems to Assist Individuals With Spinal Cord Injury

NCT03773692 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-12-12

No results posted yet for this study

Summary

The objective of this study is to develop algorithms that incorporate each individual's automatically detected physical activity (PA) level and a clinician's PA level recommendation to provide a smartphone application that helps a person set safe and highly personalized PA goals. By adapting the goals in real-time based on the person's actual behavior, the system aims to keep the individual feeling positive and motivated towards a change in the PA behavior.

Conditions

  • Spinal Cord Injuries

Interventions

BEHAVIORAL

Passive feedback and JITAI

Second Phase - PA Level Feedback A PA recommendation handout based on PA guidelines for individuals with SCI will be provided. Participants continue to use the same sensing equipment as in phase one (baseline). The equipment consists of a smartwatch, a smartphone, and a wheel rotation monitor. Participants can view their feedback whenever they want, but will not be prompted with the information. Third Phase - PA Level Feedback and Just-in-time Adaptive Intervention (JITAI) The third phase of the study will be similar to the second phase of the study, but with an additional JITAI component. The JITAI component of the study will include providing proactively-prompted, real-time feedback through the smartphone and smartwatch when the participant performs a bout of moderate PA.

Sponsors & Collaborators

  • The Craig H. Neilsen Foundation

    collaborator OTHER

  • Northeastern University

    collaborator OTHER

  • Magee Rehabilitation Hospital, Jefferson Health

    collaborator UNKNOWN

  • MossRehab: Einstein Healthcare Network

    collaborator UNKNOWN

  • Temple University

    lead OTHER

Principal Investigators

  • Shivayogi V Hiremath, PhD · Temple University

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-31
Primary Completion
2018-11-21
Completion
2018-11-21

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03773692 on ClinicalTrials.gov